NDC11 63323067305
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 63323-0673-05 | 63323-0673 |
| 63323-0673-5 | 63323-0673 |
| 63323-673-05 | 63323-673 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Palonosetron | PALONOSETRON | Fresenius Kabi USA, LLC | b93fae8e-2b76-421e-95bc-ba08c211a7ea | 2021-01-11 | Warnings, Adverse reactions | 63323-673 |
| PALONOSETRON | PALONOSETRON | Fresenius Kabi USA, LLC | 9132366b-b808-46c9-b167-c1900bc116b3 | 2020-12-29 | Warnings, Adverse reactions | 63323-673-05 63323-673 63323067305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.